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Gut bacteria alleviate smoking-related NASH by degrading gut nicotine.
Chen, Bo; Sun, Lulu; Zeng, Guangyi; Shen, Zhe; Wang, Kai; Yin, Limin; Xu, Feng; Wang, Pengcheng; Ding, Yong; Nie, Qixing; Wu, Qing; Zhang, Zhiwei; Xia, Jialin; Lin, Jun; Luo, Yuhong; Cai, Jie; Krausz, Kristopher W; Zheng, Ruimao; Xue, Yanxue; Zheng, Ming-Hua; Li, Yang; Yu, Chaohui; Gonzalez, Frank J; Jiang, Changtao.
Afiliação
  • Chen B; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Sun L; Center of Basic Medical Research, Institute of Medical Innovation and Research, Third Hospital, Peking University, Beijing, China.
  • Zeng G; Center for Obesity and Metabolic Disease Research, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Shen Z; The Key Laboratory of Molecular Cardiovascular Science, Peking University, Ministry of Education, Beijing, China.
  • Wang K; Laboratory of Metabolism, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Yin L; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Xu F; Center of Basic Medical Research, Institute of Medical Innovation and Research, Third Hospital, Peking University, Beijing, China.
  • Wang P; Center for Obesity and Metabolic Disease Research, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Ding Y; The Key Laboratory of Molecular Cardiovascular Science, Peking University, Ministry of Education, Beijing, China.
  • Nie Q; Department of Gastroenterology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
  • Wu Q; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Zhang Z; Center of Basic Medical Research, Institute of Medical Innovation and Research, Third Hospital, Peking University, Beijing, China.
  • Xia J; Center for Obesity and Metabolic Disease Research, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Lin J; The Key Laboratory of Molecular Cardiovascular Science, Peking University, Ministry of Education, Beijing, China.
  • Luo Y; Department of Pharmacology, State Key Laboratory of Medical Neurobiology, Key Laboratory of Metabolism and Molecular Medicine, the Ministry of Education, School of Basic Medical Science, Fudan University, Shanghai, China.
  • Cai J; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Krausz KW; Center of Basic Medical Research, Institute of Medical Innovation and Research, Third Hospital, Peking University, Beijing, China.
  • Zheng R; Center for Obesity and Metabolic Disease Research, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Xue Y; The Key Laboratory of Molecular Cardiovascular Science, Peking University, Ministry of Education, Beijing, China.
  • Zheng MH; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Li Y; Center of Basic Medical Research, Institute of Medical Innovation and Research, Third Hospital, Peking University, Beijing, China.
  • Yu C; Center for Obesity and Metabolic Disease Research, School of Basic Medical Sciences, Peking University, Beijing, China.
  • Gonzalez FJ; The Key Laboratory of Molecular Cardiovascular Science, Peking University, Ministry of Education, Beijing, China.
  • Jiang C; Department of Physiology and Pathophysiology, School of Basic Medical Sciences, Peking University, Beijing, China.
Nature ; 610(7932): 562-568, 2022 10.
Article em En | MEDLINE | ID: mdl-36261549
ABSTRACT
Tobacco smoking is positively correlated with non-alcoholic fatty liver disease (NAFLD)1-5, but the underlying mechanism for this association is unclear. Here we report that nicotine accumulates in the intestine during tobacco smoking and activates intestinal AMPKα. We identify the gut bacterium Bacteroides xylanisolvens as an effective nicotine degrader. Colonization of B. xylanisolvens reduces intestinal nicotine concentrations in nicotine-exposed mice, and it improves nicotine-exacerbated NAFLD progression. Mechanistically, AMPKα promotes the phosphorylation of sphingomyelin phosphodiesterase 3 (SMPD3), stabilizing the latter and therefore increasing intestinal ceramide formation, which contributes to NAFLD progression to non-alcoholic steatohepatitis (NASH). Our results establish a role for intestinal nicotine accumulation in NAFLD progression and reveal an endogenous bacterium in the human intestine with the ability to metabolize nicotine. These findings suggest a possible route to reduce tobacco smoking-exacerbated NAFLD progression.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Hepatopatia Gordurosa não Alcoólica / Fumar Tabaco / Intestinos / Nicotina Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Hepatopatia Gordurosa não Alcoólica / Fumar Tabaco / Intestinos / Nicotina Tipo de estudo: Etiology_studies / Prognostic_studies Limite: Animals / Humans Idioma: En Revista: Nature Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China